DisGeNET - a database of gene-disease associations

List of shared variants

Amyloidosis, C0002726

Disease: Alzheimer's Disease

Source: ALL

Results per page

Gene

Disease

Variant

Source

DSI _v

DPI _v

pLI

Consequence

AF_EXOME

AF_GENOME

Variant	Gene	DSI _v	DPI _v	Chr	Position	Consequence	Alleles	Class	AF EXOME	AF GENOME	Num. diseases
rs6265	BDNF ; BDNF-AS	0.436	0.760	11	27658369	missense variant	C/T	snv	0.19	0.15	272
rs759834365	BDNF-AS ; BDNF	0.448	0.760	11	27658456	missense variant	C/T	snv	1.2E-05		237
rs1045642	ABCB1	0.456	0.840	7	87509329	synonymous variant	A/G;T	snv	0.50		214
rs61752717	MEFV	0.583	0.840	16	3243407	missense variant	T/A;C	snv	2.8E-04		72
rs28933979	TTR	0.587	0.600	18	31592974	missense variant	G/A;C	snv	1.0E-04		70
rs121912438	SOD1	0.605	0.520	21	31667299	missense variant	G/A;C;T	snv	1.2E-05; 8.0E-06		58
rs63750231	PSEN1	0.689	0.160	14	73198100	missense variant	A/C;G	snv			23
rs781049584	APP	0.724	0.280	21	26021917	missense variant	T/G	snv	8.2E-06	7.0E-06	18
rs572842823	APP	0.763	0.160	21	25897626	missense variant	T/A;G	snv			11
rs17070145	WWC1	0.790	0.120	5	168418786	intron variant	C/T	snv		0.43	10
rs371425292	APP	0.763	0.160	21	25897627	missense variant	C/A;T	snv	8.0E-06		10
rs63750526	PSEN1	0.776	0.160	14	73192832	missense variant	C/A	snv			10
rs63750847	APP	0.790	0.120	21	25897620	missense variant	C/T	snv	4.5E-04	3.0E-04	8
rs63751039	APP	0.776	0.200	21	25891855	missense variant	T/C	snv			8
rs6656401	CR1	0.776	0.200	1	207518704	intron variant	A/G;T	snv			8
rs744373		0.851	0.160	2	127137039	downstream gene variant	A/G	snv		0.35	8
rs73069071	IAPP ; SLCO1A2	0.807	0.240	12	21357370	intron variant	T/C	snv		0.14	6
rs2234246	TREM1	0.827	0.240	6	41276002	3 prime UTR variant	C/T	snv		0.44	5
rs2279590	CLU	0.851	0.200	8	27598736	non coding transcript exon variant	T/C	snv		0.69	5
rs9331888	CLU ; MIR6843	0.827	0.200	8	27611345	5 prime UTR variant	C/G	snv	0.35	0.28	5
rs950592627	APP	0.827	0.200	21	26090015	missense variant	G/C	snv		7.0E-06	5
rs763852444	APP	0.882	0.120	21	26112127	missense variant	G/C	snv	4.0E-06		3
rs10097505	ARC	0.925	0.120	8	142612823	3 prime UTR variant	G/A	snv		0.47	2
rs13031703	LOC105373605	0.925	0.120	2	127129099	intergenic variant	C/T	snv		0.11	2
rs200538373	ABCA7	0.925	0.120	19	1061893	splice region variant	G/A;C	snv	2.5E-03		2